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Lupus Podocytopathy: A Rare Cause of Nephrotic Syndrome in Patients with Systemic Lupus Erythematosus

被引：0
|
作者：
Khan, Omair [1 ]
Mohammadrezaei, Fatemeh [1 ]
Aslam, Sadia [1 ]
Khan, Mohammad H. [2 ]
Wilches, Rita D. M. [1 ]
Singh, Sehajpreet [1 ]
Scheers-Masters, Joshua [1 ]
机构：
[1] Maimonides Hosp, Brooklyn, NY USA
[2] Shifa Coll Med, Islamabad, Pakistan
来源：
JOURNAL OF COMMUNITY HOSPITAL INTERNAL MEDICINE PERSPECTIVES | 2023年 / 13卷 / 05期
关键词：
Lupus podocytopathy; Nephrotic syndrome; SLE; Lupus nephritis; Minimal change disease; NEPHRITIS; THERAPY;
D O I：
10.55729/2000-9666.1218
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Lupus podocytopathy, a unique form of lupus nephritis, mimics minimal change disease (MCD) or primary focal segmental glomerulosclerosis (FSGS) and represents approximately 1% of lupus nephritis biopsies. Lupus podocytop-athy is characterized by diffuse epithelial cell foot process effacement without immune complex deposition or with only mesangial immune complex deposition. We present the case of a young woman with systemic lupus erythematosus (SLE) who presented with nephrotic syndrome and acute kidney injury (AKI) and was subsequently diagnosed with lupus podocytopathy.
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收藏
页码：57 / 60
页数：6
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